Works matching IS 03406717 AND DT 2019 AND VI 138 AND IP 4

Results: 10

On the relationship between the heritability and the attributable fraction.

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 425, doi. 10.1007/s00439-019-02006-8

By:

Dahlqwist, Elisabeth;
Magnusson, Patrik K. E.;
Pawitan, Yudi;
Sjölander, Arvid

Publication type:

Article

Genetic kinship and admixture in Iron Age Scytho-Siberians.

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 411, doi. 10.1007/s00439-019-02002-y

By:

Mary, Laura;
Zvénigorosky, Vincent;
Kovalev, Alexey;
Gonzalez, Angéla;
Fausser, Jean-Luc;
Jagorel, Florence;
Kilunovskaya, Marina;
Semenov, Vladimir;
Crubézy, Eric;
Ludes, Bertrand;
Keyser, Christine

Publication type:

Article

Estimating carrier frequencies of newborn screening disorders using a whole-genome reference panel of 3552 Japanese individuals.

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 389, doi. 10.1007/s00439-019-01998-7

By:

Yamaguchi-Kabata, Yumi;
Yasuda, Jun;
Uruno, Akira;
Shimokawa, Kazuro;
Koshiba, Seizo;
Suzuki, Yoichi;
Fuse, Nobuo;
Kawame, Hiroshi;
Tadaka, Shu;
Nagasaki, Masao;
Kojima, Kaname;
Katsuoka, Fumiki;
Kumada, Kazuki;
Tanabe, Osamu;
Tamiya, Gen;
Yaegashi, Nobuo;
Kinoshita, Kengo;
Yamamoto, Masayuki;
Kure, Shigeo

Publication type:

Article

The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus.

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 375, doi. 10.1007/s00439-019-01994-x

By:

Schlicht, Kristina;
Nyczka, Piotr;
Caliebe, Amke;
Freitag-Wolf, Sandra;
Claringbould, Annique;
Franke, Lude;
Võsa, Urmo;
Kardia, Sharon L. R.;
Smith, Jennifer A.;
Zhao, Wei;
Gieger, Christian;
Peters, Annette;
Prokisch, Holger;
Strauch, Konstantin;
Baurecht, Hansjörg;
Weidinger, Stephan;
Rosenstiel, Philip;
Hütt, Marc-Thorsten;
Knecht, Carolin;
Szymczak, Silke

Publication type:

Article

Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders.

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 363, doi. 10.1007/s00439-019-01993-y

By:

Beaumont, Marie;
Akloul, Linda;
Carré, Wilfrid;
Quélin, Chloé;
Journel, Hubert;
Pasquier, Laurent;
Fradin, Mélanie;
Odent, Sylvie;
Hamdi-Rozé, Houda;
Watrin, Erwan;
Dupé, Valérie;
Dubourg, Christèle;
David, Véronique

Publication type:

Article

Molybdenum cofactor deficiency type B knock-in mouse models carrying patient-identical mutations and their rescue by singular AAV injections.

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 355, doi. 10.1007/s00439-019-01992-z

By:

Reiss, Jochen

Publication type:

Article

Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 339, doi. 10.1007/s00439-019-01991-0

By:

Musolf, Anthony M.;
Simpson, Claire L.;
Alexander, Theresa A.;
Portas, Laura;
Murgia, Federico;
Ciner, Elise B.;
Stambolian, Dwight;
Bailey-Wilson, Joan E.

Publication type:

Article

Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation.

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 327, doi. 10.1007/s00439-019-01990-1

By:

Zhou, Zhou;
Ni, Caixia;
Wu, Ling;
Chen, Biaobang;
Xu, Yao;
Zhang, Zhihua;
Mu, Jian;
Li, Bin;
Yan, Zheng;
Fu, Jing;
Wang, Wenjing;
Zhao, Lin;
Dong, Jie;
Sun, Xiaoxi;
Kuang, Yanping;
Sang, Qing;
Wang, Lei

Publication type:

Article

Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer.

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 307, doi. 10.1007/s00439-019-01989-8

By:

Bien, Stephanie A.;
Su, Yu-Ru;
Conti, David V.;
Harrison, Tabitha A.;
Qu, Conghui;
Guo, Xingyi;
Lu, Yingchang;
Albanes, Demetrius;
Auer, Paul L.;
Banbury, Barbara L.;
Berndt, Sonja I.;
Bézieau, Stéphane;
Brenner, Hermann;
Buchanan, Daniel D.;
Caan, Bette J.;
Campbell, Peter T.;
Carlson, Christopher S.;
Chan, Andrew T.;
Chang-Claude, Jenny;
Chen, Sai

Publication type:

Article

How to increase our belief in discovered statistical interactions via large-scale association studies?

Published in:

Human Genetics, 2019, v. 138, n. 4, p. 293, doi. 10.1007/s00439-019-01987-w

By:

Van Steen, K.;
Moore, J. H.

Publication type:

Article